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  • Validation and method transfer team as and when required. - Take Care of OOS, OOT justification reports, deviations and its assessments by roots cause investigation and CAPA. - Set up , manage and maintain the analytical laboratory by ensuring proper care/use of instruments, updating SOPs, risk assessment

  • Validation and method transfer team as and when required. - Take Care of OOS, OOT justification reports, deviations and its assessments by roots cause investigation and CAPA. - Set up , manage and maintain the analytical laboratory by ensuring proper care/use of instruments, updating SOPs, risk assessment

  • Validation and method transfer team as and when required. - Take Care of OOS, OOT justification reports, deviations and its assessments by roots cause investigation and CAPA. - Set up , manage and maintain the analytical laboratory by ensuring proper care/use of instruments, updating SOPs, risk assessment

  • Validation and method transfer team as and when required. - Take Care of OOS, OOT justification reports, deviations and its assessments by roots cause investigation and CAPA. - Set up , manage and maintain the analytical laboratory by ensuring proper care/use of instruments, updating SOPs, risk assessment

  • Validation and method transfer team as and when required. - Take Care of OOS, OOT justification reports, deviations and its assessments by roots cause investigation and CAPA. - Set up , manage and maintain the analytical laboratory by ensuring proper care/use of instruments, updating SOPs, risk assessment

  • Validation and method transfer team as and when required. - Take Care of OOS, OOT justification reports, deviations and its assessments by roots cause investigation and CAPA. - Set up , manage and maintain the analytical laboratory by ensuring proper care/use of instruments, updating SOPs, risk assessment

  • 1) Production schedule, co-ordination for Raw material arrangements and executer of planned quantities. 2) Ensure the changes to vendor / processes / equipment / procedures. 3) Ensure the investigation of deviation s, complaints based on QA Communi

  • 1) Production schedule, co-ordination for Raw material arrangements and executer of planned quantities. 2) Ensure the changes to vendor / processes / equipment / procedures. 3) Ensure the investigation of deviation s, complaints based on QA Communi

  • 1) Production schedule, co-ordination for Raw material arrangements and executer of planned quantities. 2) Ensure the changes to vendor / processes / equipment / procedures. 3) Ensure the investigation of deviation s, complaints based on QA Communi

  • 1) Production schedule, co-ordination for Raw material arrangements and executer of planned quantities. 2) Ensure the changes to vendor / processes / equipment / procedures. 3) Ensure the investigation of deviation s, complaints based on QA Communi

  • 1) Production schedule, co-ordination for Raw material arrangements and executer of planned quantities. 2) Ensure the changes to vendor / processes / equipment / procedures. 3) Ensure the investigation of deviation s, complaints based on QA Communi

  • Position will be responsible for Preparation, review and submission of Drug Master Files in eCTD format for the regions US, EU and Health Canada through ESG and CESP and experience in ROW markets. Preparation and submission of self-identification, addition of importers and NDC labels to USFDA ...

  • Position will be responsible for Preparation, review and submission of Drug Master Files in eCTD format for the regions US, EU and Health Canada through ESG and CESP and experience in ROW markets. Preparation and submission of self-identification, addition of importers and NDC labels to USFDA ...

  • Position will be responsible for Preparation, review and submission of Drug Master Files in eCTD format for the regions US, EU and Health Canada through ESG and CESP and experience in ROW markets. Preparation and submission of self-identification, addition of importers and NDC labels to USFDA ...

  • Position will be responsible for Preparation, review and submission of Drug Master Files in eCTD format for the regions US, EU and Health Canada through ESG and CESP and experience in ROW markets. Preparation and submission of self-identification, addition of importers and NDC labels to USFDA ...

  • Manage all APIs and Track them if its working well and make dashboards (only Visual Studio mandate). 4 year degree in a College or University 3+ years of experience content permission and authorization processes 3+ years of supporting APIs Basic understanding of object oriented programming

  • Manage all APIs and Track them if its working well and make dashboards (only Visual Studio mandate). 4 year degree in a College or University 3+ years of experience content permission and authorization processes 3+ years of supporting APIs Basic understanding of object oriented programming

  • Manage all APIs and Track them if its working well and make dashboards (only Visual Studio mandate). 4 year degree in a College or University 3+ years of experience content permission and authorization processes 3+ years of supporting APIs Basic understanding of object oriented programming

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